Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan
Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
J Pharmacol Exp Ther. 2022 Jan;380(1):26-33. doi: 10.1124/jpet.121.000686. Epub 2021 Nov 2.
Thymic stromal lymphopoietin (TSLP), positioned at the top of the inflammatory cascade, is a key regulator that enhances allergic inflammatory responses by activating T helper type 2 cells, Group 2 innate lymphoid cells (ILC2), and myeloid dendritic cells (mDCs) via the TSLP receptor (TSLPR). We evaluated the inhibitory effects of ASP7266, a novel recombinant fully human IgG monoclonal antibody against TSLPR, on TSLP signaling and inflammation. The inhibitory effects of ASP7266 and the control antibody tezepelumab on TSLP and TSLPR interactions were investigated using a proliferation assay with TSLP stimulation and a chemokine production assay. The pharmacological effects of ASP7266 were investigated by examining differentiation of naive CD4 T cells, ILC2 cytokine production, and ascaris extract-induced skin allergic reaction in cynomolgus monkeys. ASP7266 potently inhibited TSLP-induced cell proliferation and C-C motif chemokine ligand 17 production. Furthermore, ASP7266 inhibited TSLP-stimulated mDC-mediated naive CD4 T-cell differentiation and interleukin 5 production by lineage-negative peripheral blood mononuclear cells, which can be considered ILC2 in vitro. In sensitized monkeys, ASP7266 completely suppressed ascaris extract-induced allergic skin reactions. Based on these results, ASP7266, a novel human therapeutic antibody against TSLPR, is a potential therapy for patients with allergic diseases. SIGNIFICANCE STATEMENT: TSLP, positioned at the top of the inflammatory cascade, plays a key role in various allergic diseases, including asthma, chronic rhinosinusitis with nasal polyposis, and atopic dermatitis. Here we show that the anti-TSLPR antibody ASP7266 exhibited excellent pharmacological activity in preclinical studies. Therefore, ASP7266 has the potential to be a promising treatment option for patients with allergic disorders.
胸腺基质淋巴细胞生成素 (TSLP) 位于炎症级联的顶端,是一种关键的调节剂,通过激活辅助性 T 细胞 2 型 (Th2 细胞)、 2 类固有淋巴样细胞 (ILC2) 和髓样树突状细胞 (mDC),增强过敏炎症反应。我们评估了新型重组人源 IgG 单克隆抗体 ASP7266 针对 TSLP 受体 (TSLPR) 的抑制作用对 TSLP 信号和炎症的影响。通过 TSLP 刺激的增殖试验和趋化因子产生试验,研究了 ASP7266 和对照抗体特泽佩鲁单抗对 TSLP 和 TSLPR 相互作用的抑制作用。通过检查幼稚 CD4 T 细胞的分化、ILC2 细胞因子的产生以及食蟹猴的寄生虫提取物诱导的皮肤过敏反应,研究了 ASP7266 的药理作用。ASP7266 强烈抑制 TSLP 诱导的细胞增殖和 C-C 基序趋化因子配体 17 的产生。此外,ASP7266 抑制 TSLP 刺激的 mDC 介导的幼稚 CD4 T 细胞分化和白细胞介素 5 的产生,在体外可被认为是 ILC2。在致敏的猴子中,ASP7266 完全抑制了寄生虫提取物诱导的过敏皮肤反应。基于这些结果,针对 TSLPR 的新型人源治疗性抗体 ASP7266 是治疗过敏疾病患者的潜在疗法。
TSLP 位于炎症级联的顶端,在各种过敏性疾病中发挥关键作用,包括哮喘、伴鼻息肉的慢性鼻-鼻窦炎和特应性皮炎。在这里,我们表明抗 TSLPR 抗体 ASP7266 在临床前研究中表现出优异的药理活性。因此,ASP7266 有可能成为治疗过敏性疾病患者的有前途的治疗选择。